WhichRecall
Class IIReported 2025-08-27

Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14.

Recalled by PFIZER INC

Reason for Recall

Lack of Assurance of Sterility.

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Recall Number
D-0591-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-08-04
Reported
2025-08-27
Distribution
U.S. Nationwide
Code Info
Lot #: LH2671, Exp. 11/30/2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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